Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_assertion evidence source_evidence_literature NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_assertion SIO_000772 20586826 NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_assertion wasDerivedFrom gad-20150221 NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_assertion wasGeneratedBy ECO_0000203 NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.